超价根二元体的金属化:分子和带视角
John S Tse1, Alicea A Leitch, Xueyang Yu
1Department of Physics and Engineering Physics, University of Saskatchewan, Saskatoon, Saskatchewan S7N 5E2, Canada.
Journal of the American Chemical Society
|March 13, 2010
概括
在高压下 (5-9 GPa) 的bistiaselenazolyl基质二元体表现出弱金属状态. 这种金属化是由分子内结构变化和分子间相互作用驱动的,导致HOMO-LUMO间隙崩和带间隙关闭.
科学领域:
- 材料科学 材料科学 材料科学
- 固态物理 固态物理
- 晶体学 晶体学是指结晶学.
背景情况:
- 贝斯蒂亚塞莱纳佐利基基二元体 ([1a](2) 被研究其电子性质.
- 了解分子材料的压力诱导金属化对于开发新的电子设备至关重要.
研究的目的:
- 为了调查压力下 [1a](2) 中弱金属状态的起源.
- 使用计算方法将结构变化与电子转换相关联.
主要方法:
- 可变压力和温度导电性测量.
- 在压力下分析晶体结构的X射线衍射.
- 密度函数理论 (DFT) 对分子和固态电子结构的计算.
主要成果:
- 在5-9 GPa.之间观察到一个弱金属状态.
- 加压会导致二极管的曲和S-Se键的收缩,这表明了电子配置开关.
- DFT计算显示HOMO-LUMO间隙减少和带间隙关闭,形成一个准金属状态.
结论:
- 在 [1a](2) 中的金属化是由分子内部结构变化 (HOMO-LUMO间隙崩) 和分子间相互作用 (带边叠加) 所导致的.
- 该研究强调了压力诱导的电子相变中的分子构造和晶体包装之间的相互作用.
相关概念视频
Radical Reactivity: Overview
3.0K
Radicals, the highly reactive species, gain stability by undergoing three different reactions. The first reaction involves a radical-radical coupling, in which a radical combines with another radical, forming a spin‐paired molecule. The second reaction is between a radical and a spin‐paired molecule, generating a new radical and a new spin‐paired molecule. The third reaction is radical decomposition in a unimolecular reaction, forming a new radical and a spin‐paired...
3.0K
Radical Reactivity: Intramolecular vs Intermolecular
2.3K
Radical reactions can occur either intermolecularly or intramolecularly. In an intermolecular radical reaction, a nucleophilic radical adds to an electrophilic alkene or vice versa. In such reactions, the radical and generally the alkene, which is also called the radical trap, are two different molecules. Additionally, for such intermolecular reactions to occur, the radical trap must be active, present in an excess concentration, and the radical starting material must have a weak...
2.3K
π Molecular Orbitals of the Allyl Radical
4.8K
Allyl radicals are three-carbon conjugated systems. They are readily formed as intermediates in halogenation reactions of alkenes involving the addition of halogen to the allylic carbon instead of the double bond. As seen in allyl cations and anions, each of the three sp2-hybridized carbon atoms in allyl radicals has an unhybridized p orbital. These orbitals combine to give three π molecular orbitals.
The allyl systems have identical molecular orbitals but differ in the number of π electrons....
The allyl systems have identical molecular orbitals but differ in the number of π electrons....
4.8K
Radicals: Electronic Structure and Geometry
5.3K
This lesson delves into the geometry of a radical, which is influenced by the electronic structure of the molecule. The principle is similar to that of a lone pair, where the unpaired electron influences the geometry at the radical center.
Accordingly, the structure of a trivalent radical lies between the geometries of carbocations and carbanions. An sp2-hybridized carbocation is trigonal planar, while an sp3-hybridized carbanion is trigonal pyramidal. Here, the difference in geometry is...
Accordingly, the structure of a trivalent radical lies between the geometries of carbocations and carbanions. An sp2-hybridized carbocation is trigonal planar, while an sp3-hybridized carbanion is trigonal pyramidal. Here, the difference in geometry is...
5.3K
Radical Formation: Overview
2.7K
A bond can be broken either by heterolytic bond cleavage to form ions or homolytic bond cleavage to yield radicals. A fishhook arrow is used to represent the motion of a single electron in homolytic bond cleavage. There are two main sources from which radicals can be formed:
Radicals from spin-paired molecules:
Radicals can be obtained from spin-paired molecules either by homolysis or electron transfer. While two radicals are formed in the former, an electron is added in the...
Radicals from spin-paired molecules:
Radicals can be obtained from spin-paired molecules either by homolysis or electron transfer. While two radicals are formed in the former, an electron is added in the...
2.7K
Radical Formation: Abstraction
4.5K
The electron of an atom can be abstracted from a compound by a relatively unstable radical to generate a new radical of relatively greater stability. For example, an initiator which forms radicals by homolysis can abstract a suitable species like a hydrogen atom or a halogen atom from a compound to generate a new radical. This ability of radicals to propagate by abstraction is a crucial feature of radical chain reactions.
Even though homolysis produces radicals, it is different from radical...
Even though homolysis produces radicals, it is different from radical...
4.5K


